Job Summary
A company is looking for a New Jersey Licensed Principal SAS Programmer.
Responsibilities
- Serve as lead programmer for assigned projects, providing statistical and programming support in clinical studies
- Design and perform quality checks on analysis datasets and reports using SAS
- Communicate with clients regarding study protocol or statistical analysis issues
Requirements
- PhD or MS degree in Statistics, Biostatistics, or related field
- 5+ years of relevant work experience in the CRO, biotech, pharmaceutical, or life sciences industry
- Familiarity with clinical trial design and regulatory guidelines (FDA/EMA, ICH/GCP)
- Experience with NDA/BLA submission activities and statistical programs such as SAS
- Understanding of Ultra Compare software and industry standards
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